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Healix Infusion Therapy, Inc. recalls fentaNYL 2750 mcg/55 mL (50 mcg/mL) in prefilled syringe, COMPOUNDED DRUG, For Institutional or Office Use Only--Not f

Recalled August 27, 2014 · FDA recall D-1554-2014 · Healix Infusion Therapy

Hazard
Lack of Assurance of Sterility: Firm received fentanyl from a supplier who recalled it because fliptop vial crimps were loose or missing. · FDA Class II
Units
220 syringes
Sold at
Texas and Georgia

Description

Lack of Assurance of Sterility: Firm received fentanyl from a supplier who recalled it because fliptop vial crimps were loose or missing.

Product
fentaNYL 2750 mcg/55 mL (50 mcg/mL) in prefilled syringe, COMPOUNDED DRUG, For Institutional or Office Use Only--Not for Resale Federal Law Prohibits Dispensing without Prescription Healix Infusion Therapy, Inc. (866) 298-4826 1075 West Park One Drive, Suite 200, Sugar Land, Texas, 77478 NDC 75901-8008-33
Manufacturer(s)
Healix Infusion Therapy, Inc.

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov

Healix Infusion Therapy, Inc. recalls fentaNYL 2750 mcg/55 mL (50 mcg/mL) in prefilled syringe, COMPOUNDED DRUG, For Institutional or Office Use Only--Not f | RecallWatchUSA